Canonical Allele Identifier: CA437323362

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855474A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137686A>C , CM000665.2:g.184137686A>C	GRCh38
NC_000003.11:g.183855474A>C , CM000665.1:g.183855474A>C	GRCh37
NC_000003.10:g.185338168A>C	NCBI36
NG_015826.1:g.7665A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000465218.3:n.410A>C
ENST00000468748.7:n.370A>C
ENST00000484154.2:n.1008A>C
ENST00000491008.6:n.1135A>C
ENST00000492226.2:n.384A>C
ENST00000492773.6:c.119A>C
ENST00000647636.1:c.387A>C	ENSP00000497505.1:p.Arg129=
ENST00000647909.1:c.387A>C	ENSP00000498164.1:p.Arg129=
ENST00000648145.1:c.155A>C
ENST00000648189.1:c.137A>C
ENST00000648256.1:c.336A>C	ENSP00000497356.1:p.Arg112=
ENST00000648314.1:c.387A>C	ENSP00000496920.1:p.Arg129=
ENST00000648599.1:c.387A>C	ENSP00000497159.1:p.Arg129=
ENST00000648630.1:c.381A>C	ENSP00000497887.1:p.Arg127=
ENST00000648682.1:c.387A>C	ENSP00000498185.1:p.Arg129=
ENST00000648882.1:c.*213A>C	ENSP00000497603.1:n.*213A>C
ENST00000648890.1:c.387A>C	ENSP00000497503.1:p.Arg129=
ENST00000648915.2:c.387A>C MANE Select	ENSP00000497160.1:p.Arg129=
ENST00000649545.1:c.121A>C
ENST00000649688.1:c.387A>C	ENSP00000497097.1:p.Arg129=
ENST00000649814.1:n.436A>C
ENST00000650244.1:c.532A>C	ENSP00000497227.1:n.532A>C
ENST00000650270.1:c.254A>C
ENST00000273783.7:c.387A>C	ENSP00000273783.3:p.Arg129=
ENST00000432982.5:c.245+1011A>C
ENST00000444495.1:c.387A>C	ENSP00000409142.1:p.Arg129=
ENST00000481054.5:n.388A>C
ENST00000491008.5:n.351A>C
ENST00000491144.5:n.735A>C
ENST00000498831.1:n.342A>C
NM_003907.2:c.387A>C	NP_003898.2:p.Arg129=
XR_924208.1:n.1338A>C
NM_003907.3:c.387A>C MANE Select	NP_003898.2:p.Arg129=
XM_011513266.3:c.-515A>C	XP_011511568.1:n.-515A>C
XR_001740352.2:n.750A>C
XR_001740353.2:n.750A>C
XR_924208.2:n.750A>C